Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,564 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,564 in last 12 months

Showing 2326123280 of 53,342 recalls

Medical DeviceApril 29, 2019· KaVo Dental Technologies LLC

Recalled Item: DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral...

The Issue: The sensor's look up calibration files were incorrectly programmed during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Inovo, Inc

Recalled Item: Inovo Single Luman Conserver Product Usage: This device is intended Recalled...

The Issue: The pressure gauge (manometer) may dislodge from the threaded...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Balloon Expandable TransFemoral System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· Cytocell Ltd.

Recalled Item: Aquarius D13S319 Plus Deletion Probe Recalled by Cytocell Ltd. Due to There...

The Issue: There is an error in the chromomap on the package insert.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: Portico Solo Re-Collapsible Access System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Re-Collapsible Access System Recalled by Terumo Medical Corporation...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 26, 2019· Advanced Pharma Inc.

Recalled Item: HYDROmorphone 20 mg/100 mL Injectable Solution Recalled by Advanced Pharma...

The Issue: Sub-potency

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2019· Advantice Health

Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters...

The Issue: Labeling: Not Elsewhere Classified: Full cases may contain canisters that...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 25, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2019· US Worldmeds LLC

Recalled Item: Revonto (dantrolene sodium for injection) Recalled by US Worldmeds LLC Due...

The Issue: Presence of Precipitate: Appearance is Out of Specification for the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2019· Advantice Health

Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters...

The Issue: Labeling: Not Elsewhere Classified: canisters incorrectly state the net...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 25, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Acyclovir Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Labeling;...

The Issue: Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 25, 2019· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product...

The Issue: Potential risk of brush detachment during cleaning. If brush detachment is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2019· ASTRA, LLC

Recalled Item: Lidar System for Erosion Flume Application Class 1 Laser Product Recalled by...

The Issue: Failure to comply event due to incorrect labeling of a class 1 laser product.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: IV KIT - SORBAVIEW IVS3475 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CAP BUNDLE KIT DYNDC2137 Recalled by Centurion Medical Products Corporation...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PEDIATRIC PICC INSERTION TRAY CVI4450 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840 Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing